Just diagnosed with Dent disease?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Dent disease, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Dent disease hub →Overview
Dent disease is a rare condition. Also known as Dent syndrome, Low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis, Renal Fanconi syndrome with nephrocalcinosis and renal stones, X-linked recessive hypercalciuric hypophosphatemic rickets, X-linked recessive nephrolithiasis. Tomeko brings together the specialists, research, clinical trials, treatments and community for Dent disease so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:1652 · OMIM 300009, 300554, 300555 · ICD-10 N25.8 · GARD 0013105
Find care for Dent disease
Authoritative references for Dent disease
Research & market landscape for Dent disease
Following Dent disease for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Dent disease — the real-world landscape behind the condition, in one place.
- Latest Dent disease research on PubMed ↗
- Recruiting Dent disease trials on ClinicalTrials.gov ↗
- Explore the Dent disease research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Dent disease and every rare condition. See how Tomeko works with industry →
Common questions
What is Dent disease?
Dent disease is a rare condition. Also known as Dent syndrome, Low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis, Renal Fanconi syndrome with nephrocalcinosis and renal stones, X-linked recessive hypercalciuric hypophosphatemic rickets, X-linked recessive nephrolithiasis. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Dent disease together in one place.
What are the symptoms of Dent disease?
Symptoms of Dent disease vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Dent disease.
How is Dent disease treated?
Treatment for Dent disease depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Dent disease, and review current options with them.
What causes Dent disease — is it genetic?
The cause and inheritance of Dent disease are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Dent disease can explain what it means for you and your family.
I was just diagnosed with Dent disease — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Dent disease, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Dent disease?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Dent disease, filtered to your area.
Are there clinical trials for Dent disease?
Tomeko shows live, recruiting studies for Dent disease from ClinicalTrials.gov on the hub.
Related conditions
Other conditions on Tomeko you may be looking for:
- Autosomal dominant distal renal tubular acidosis
- Autosomal dominant proximal renal tubular acidosis
- Autosomal dominant pseudohypoaldosteronism type 1
- Autosomal recessive distal renal tubular acidosis
- Autosomal recessive proximal renal tubular acidosis
- C3 glomerulonephritis
- Collagen type III glomerulopathy
- Complement 3 glomerulopathy